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. Author manuscript; available in PMC: 2009 Jul 23.
Published in final edited form as: J Am Chem Soc. 2008 Jun 25;130(29):9214–9215. doi: 10.1021/ja803094u

Table 3.

Diels-Alder Reactions of 5 and Dienes

entry diene product conditiona yield(%)b
1 graphic file with name nihms-83440-t0004.jpg graphic file with name nihms-83440-t0005.jpg A
B
97c
67c
2 graphic file with name nihms-83440-t0006.jpg graphic file with name nihms-83440-t0007.jpg A
B
97d
65d
3 graphic file with name nihms-83440-t0008.jpg graphic file with name nihms-83440-t0009.jpg A 99
4 graphic file with name nihms-83440-t0010.jpg graphic file with name nihms-83440-t0011.jpg A 97c,e
5 graphic file with name nihms-83440-t0012.jpg graphic file with name nihms-83440-t0013.jpg A 96c
6 graphic file with name nihms-83440-t0014.jpg graphic file with name nihms-83440-t0015.jpg A 55c
a

Condition A: 10/10/60/10 mol% CoI2/8/ZnI2/Bu4NBH4, 40°C; condition B: 60/10 mol% ZnI2/Bu4NBH4, 40°C, see Supporting Information.

b

Isolated yields.

c

Single regioisomer.

d

Single endo isomer.

e

1.5:1 exo/endo ratio.